A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607184



Internal ID6647426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151761590..151765474hg38UCSC Ensembl
Innerchr5:151761625..151765439hg38UCSC Ensembl
Outerchr5:151761555..151765509hg38UCSC Ensembl
chr5:151141151..151145035hg19UCSC Ensembl
Innerchr5:151141186..151145000hg19UCSC Ensembl
Outerchr5:151141116..151145070hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383885
hg193885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12101075, essv12101074
SamplesHG00115, HG00116
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607184
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer